Summary | |
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Symbol | MCC |
Name | mutated in colorectal cancers |
Aliases | MCC1; Protein MCC; Colorectal mutant cancer protein |
Chromosomal Location | 5q21-q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Basic function annotation. > Subcellular Location, Domain and Function > Gene Ontology > KEGG and Reactome Pathway |
Subcellular Location | Cell membrane. Cell projection, lamellipodium. Nucleus Cytoplasm Note=Colocalizes with actin at the leading edge of polarized cells. |
Domain |
PF10506 PDZ domain of MCC-2 bdg protein for Usher syndrome |
Function |
Candidate for the putative colorectal tumor suppressor gene located at 5q21. Suppresses cell proliferation and the Wnt/b-catenin pathway in colorectal cancer cells. Inhibits DNA binding of b-catenin/TCF/LEF transcription factors. Involved in cell migration independently of RAC1, CDC42 and p21-activated kinase (PAK) activation (PubMed:18591935, PubMed:19555689, PubMed:22480440). Represses the beta-catenin pathway (canonical Wnt signaling pathway) in a CCAR2-dependent manner by sequestering CCAR2 to the cytoplasm, thereby impairing its ability to inhibit SIRT1 which is involved in the deacetylation and negative regulation of beta-catenin (CTNB1) transcriptional activity (PubMed:24824780). |
Biological Process |
GO:0001667 ameboidal-type cell migration GO:0010631 epithelial cell migration GO:0010632 regulation of epithelial cell migration GO:0010633 negative regulation of epithelial cell migration GO:0016055 Wnt signaling pathway GO:0030111 regulation of Wnt signaling pathway GO:0030178 negative regulation of Wnt signaling pathway GO:0030336 negative regulation of cell migration GO:0040013 negative regulation of locomotion GO:0050673 epithelial cell proliferation GO:0050678 regulation of epithelial cell proliferation GO:0050680 negative regulation of epithelial cell proliferation GO:0051271 negative regulation of cellular component movement GO:0060070 canonical Wnt signaling pathway GO:0060828 regulation of canonical Wnt signaling pathway GO:0090090 negative regulation of canonical Wnt signaling pathway GO:0090130 tissue migration GO:0090132 epithelium migration GO:0198738 cell-cell signaling by wnt GO:2000146 negative regulation of cell motility |
Molecular Function | - |
Cellular Component |
GO:0030027 lamellipodium GO:0031252 cell leading edge |
KEGG | - |
Reactome | - |
Summary | |
---|---|
Symbol | MCC |
Name | mutated in colorectal cancers |
Aliases | MCC1; Protein MCC; Colorectal mutant cancer protein |
Chromosomal Location | 5q21-q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | Literatures that report relations between MCC and anti-tumor immunity. The specific mechanism were also collected if the literature reports that a gene specifically promotes or inhibits the infiltration or function of T/NK cells. |
There is no record. |
Summary | |
---|---|
Symbol | MCC |
Name | mutated in colorectal cancers |
Aliases | MCC1; Protein MCC; Colorectal mutant cancer protein |
Chromosomal Location | 5q21-q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | High-throughput screening data (e.g. CRISPR-Cas9, shRNA and RNAi) for T cell-mediated killing. Genetic screen techniques can identify mechanisms of tumor cell resistance (e.g., PTPN2) and sensitivity (e.g., APLNR) to killing by cytotoxic T cells, the central effectors of anti-tumor immunity. After comprehensively searching, eight groups of screening data sets were collected in the current database. In this tab, users can check whether their selected genes cause resistance or increase sensitivity to T cell-mediated killing in various data sets. |
> High-throughput Screening
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Statistical results of MCC in screening data sets for detecting immune reponses.
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Summary | |
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Symbol | MCC |
Name | mutated in colorectal cancers |
Aliases | MCC1; Protein MCC; Colorectal mutant cancer protein |
Chromosomal Location | 5q21-q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Transcriptomic and genomic profiling of pre-treated tumor biopsies from responders and non-responders to immunotherapy. These data were used to identify signatures and mechanisms of response to checkpoint blockade (e.g., anti-PDL1 and anti-PD1). One example is that mutations in the gene PBRM1 benefit clinical survival of patients with clear cell renal cell carcinoma. After comprehensively searching, we collected 5 and 6 of transcriptomic and genomic data sets, respectively. In this tab, users can check whether their selected genes have significant difference of expression or mutation between responders and non-responders in various data sets. > Expression difference between responders and non-responders > Mutation difference between responders and non-responders |
Points in the above scatter plot represent the expression difference of MCC in various data sets.
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Points in the above scatter plot represent the mutation difference of MCC in various data sets.
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Summary | |
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Symbol | MCC |
Name | mutated in colorectal cancers |
Aliases | MCC1; Protein MCC; Colorectal mutant cancer protein |
Chromosomal Location | 5q21-q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of MCC. The immune-related signatures of 28 TIL types from Charoentong's study, which can be viewed in the download page. For each cancer type, the relative abundance of TILs were inferred by using gene set variation analysis (GSVA) based on gene expression profile. In this tab, users can examine which kinds of TILs might be regulated by the current gene. |
Summary | |
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Symbol | MCC |
Name | mutated in colorectal cancers |
Aliases | MCC1; Protein MCC; Colorectal mutant cancer protein |
Chromosomal Location | 5q21-q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of MCC. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by MCC. > Immunoinhibitor > Immunostimulator > MHC molecule |
Summary | |
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Symbol | MCC |
Name | mutated in colorectal cancers |
Aliases | MCC1; Protein MCC; Colorectal mutant cancer protein |
Chromosomal Location | 5q21-q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of MCC. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene. > Chemokine > Receptor |
Summary | |
---|---|
Symbol | MCC |
Name | mutated in colorectal cancers |
Aliases | MCC1; Protein MCC; Colorectal mutant cancer protein |
Chromosomal Location | 5q21-q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Distribution of MCC expression across immune and molecular subtypes. > Immune subtype > Molecular subtype |
Summary | |
---|---|
Symbol | MCC |
Name | mutated in colorectal cancers |
Aliases | MCC1; Protein MCC; Colorectal mutant cancer protein |
Chromosomal Location | 5q21-q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Associations between MCC and clinical features. > Overall survival analysis > Cancer stage > Tumor grade |